Whole genome sequencing and inheritance-based variant filtering as a tool for unraveling missing heritability in pediatric cancer-Reference-Cited by-同舟云学术

Whole genome sequencing and inheritance-based variant filtering as a tool for unraveling missing heritability in pediatric cancer

Published:2022-07-25 Issue:4 Volume:40 Page:326-340
ISSN:0888-0018
Container-title:Pediatric Hematology and Oncology
language:en
Short-container-title:Pediatric Hematology and Oncology

Author:

Derpoorter Charlotte¹²³^ORCID,Van Paemel Ruben¹³^ORCID,Vandemeulebroecke Katrien¹²³^ORCID,Vanhooren Jolien¹²³^ORCID,De Wilde Bram¹²³^ORCID,Laureys Geneviève¹²³,Lammens Tim¹²³^ORCID

Affiliation:

1. Department of Pediatric Hematology-Oncology and Stem Cell Transplantation, Ghent University Hospital, Ghent, Belgium

2. Department of Internal Medicine and Pediatrics, Ghent University, Ghent, Belgium

3. Cancer Research Institute Ghent, Ghent, Belgium

Funder

Belgian Foundation

vzw Kinderkankerfonds

Publisher

Informa UK Limited

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

https://www.tandfonline.com/doi/pdf/10.1080/08880018.2022.2101723

Reference53 articles.

1. Germline Mutations in Predisposition Genes in Pediatric Cancer

2. Pediatric Cancer Predisposition and Surveillance: An Overview, and a Tribute to Alfred G. Knudson Jr

3. Realizing the promise of cancer predisposition genes

4. A Systematic Literature Review of Whole Exome and Genome Sequencing Population Studies of Genetic Susceptibility to Cancer

5. Nationwide germline whole genome sequencing of 198 consecutive pediatric cancer patients reveals a high incidence of cancer prone syndromes

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